Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TACTCGTGTCCCTCACACACTCACC[A/G]GAGCACCCGCAGCACAGAGCCAGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612793 MIM: 173320 | ||||||||||||||||||||
Literature Links: |
PTDSS2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
PTDSS2 - phosphatidylserine synthase 2 | ||||||
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There are no transcripts associated with this gene. |
RNH1 - ribonuclease/angiogenin inhibitor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002939.3 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_002930.2 | |
NM_203383.1 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_976317.1 | |
NM_203384.1 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_976318.1 | |
NM_203385.1 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_976319.1 | |
NM_203386.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_976320.1 | |
NM_203387.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_976321.1 | |
NM_203388.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_976322.1 | |
NM_203389.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | NP_976323.1 | |
XM_011520255.1 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518557.1 | |
XM_011520257.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518559.1 | |
XM_011520258.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518560.1 | |
XM_011520259.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518561.1 | |
XM_011520260.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518562.1 | |
XM_011520261.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518563.1 | |
XM_011520262.2 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518564.1 | |
XM_011520263.1 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_011518565.1 | |
XM_017018106.1 | 1266 | Missense Mutation | CGG,TGG | R,W 376 | XP_016873595.1 |